# Claritec Company – FDA Inspection, Jul 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/claritec-company/699aab96-2fc4-4022-b7d4-5aa643b0fdc2
Source feed: FDA_Inspections

> FDA inspection 842372 of Claritec Company, July 25, 2013. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 842372
- Company Name: Claritec Company
- Inspection Date: 2013-07-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 659539 - 2010-04-26

Company: https://www.keypedia.com/companies/claritec-company/bda8f891-0de9-4504-bcfd-b3d617c3f17b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7